List of variants in gene combination ASTN2, TRIM32 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.558G>C (p.Gln186His)	rs117599771	0.00183
NM_012210.4(TRIM32):c.1222C>T (p.Arg408Cys)	rs3747835	0.00113
NM_012210.4(TRIM32):c.276C>T (p.Ser92=)	rs140589523	0.00051
NM_012210.4(TRIM32):c.770C>G (p.Thr257Arg)	rs3747834	0.00017
NM_012210.4(TRIM32):c.330A>G (p.Gln110=)	rs770015462	0.00011
NM_012210.4(TRIM32):c.409C>T (p.Pro137Ser)	rs200997003	0.00011
NM_012210.4(TRIM32):c.366C>G (p.Pro122=)	rs137947083	0.00009
NM_012210.4(TRIM32):c.238C>T (p.Leu80=)	rs760820148	0.00007
NM_012210.4(TRIM32):c.1416A>G (p.Pro472=)	rs374136376	0.00006
NM_012210.4(TRIM32):c.987G>A (p.Pro329=)	rs760513760	0.00006
NM_012210.4(TRIM32):c.1275T>C (p.Asp425=)	rs150813870	0.00005
NM_012210.4(TRIM32):c.1458C>T (p.Thr486=)	rs141965401	0.00005
NM_012210.4(TRIM32):c.1134C>T (p.Tyr378=)	rs776448126	0.00004
NM_012210.4(TRIM32):c.1609C>T (p.Leu537=)	rs139275673	0.00004
NM_012210.4(TRIM32):c.201T>C (p.Ile67=)	rs780799984	0.00004
NM_012210.4(TRIM32):c.265G>A (p.Ala89Thr)	rs539376933	0.00004
NM_012210.4(TRIM32):c.339G>C (p.Arg113=)	rs150477945	0.00004
NM_012210.4(TRIM32):c.501G>A (p.Lys167=)	rs200085883	0.00004
NM_012210.4(TRIM32):c.-5G>A	rs774975492	0.00003
NM_012210.4(TRIM32):c.1140C>T (p.Thr380=)	rs142715198	0.00002
NM_012210.4(TRIM32):c.1530A>G (p.Leu510=)	rs145728860	0.00002
NM_012210.4(TRIM32):c.370C>T (p.Arg124Trp)	rs572052810	0.00002
NM_012210.4(TRIM32):c.1161C>T (p.Val387=)	rs751224092	0.00001
NM_012210.4(TRIM32):c.1326T>A (p.Ile442=)	rs1372713940	0.00001
NM_012210.4(TRIM32):c.1383C>T (p.Cys461=)	rs200244154	0.00001
NM_012210.4(TRIM32):c.1386G>A (p.Val462=)	rs762905941	0.00001
NM_012210.4(TRIM32):c.69C>T (p.Cys23=)	rs575633576	0.00001
NM_012210.4(TRIM32):c.99T>C (p.Arg33=)	rs1057202035	0.00001
NM_012210.4(TRIM32):c.-6A>G
NM_012210.4(TRIM32):c.153A>G (p.Leu51=)	rs1413028401
NM_012210.4(TRIM32):c.1710G>A (p.Ser570=)	rs555217187
NM_012210.4(TRIM32):c.319C>T (p.Leu107=)	rs886042410
NM_012210.4(TRIM32):c.633T>C (p.Ala211=)	rs753960738
NM_012210.4(TRIM32):c.757C>T (p.Leu253=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.